Role of the leukemia-associated transcription factor STAT3 in platelet physiology

被引:18
|
作者
Vassilev, AO [1 ]
Lorenz, DR [1 ]
Tibbles, HE [1 ]
Uckun, FM [1 ]
机构
[1] Parker Hughes Inst, Parker Hughes Canc Ctr, Dept Biochem, St Paul, MN 55113 USA
关键词
STAT3; thrombopoietin; mitochondria; transcription factor; platelets;
D O I
10.1080/1042819022386716
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Actinomycin D, a transcriptional inhibitor, was found to inhibit platelet potentiation by thrombopoietin (TPO), suggesting that TPO stimulation of platelets involves mitochondrial transcription. We sought to determine a possible role for leukemia-associated signal transducers and activators of transcription (STAT) proteins as mitochondrial transcription factors, focusing specifically on STAT3 in human platelets. We found TPO stimulation of platelets activated STAT3 in vitro, that STAT3 was present in platelet mitochondrial-rich fractions as determined by Western Blot analysis and was capable of binding to the regulatory D-loop region of human mitochondrial DNA upon activation. These results suggest that platelet signaling pathways activated by TPO may affect mitochondrial transcription via activation of STAT3.
引用
收藏
页码:1461 / 1467
页数:7
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